HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257792Generated: November 2, 2026
Hydrochloric Acid → (6-Methylpyridin-3-yl)methanol
https://huagongshe.com/reaction/257792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl 6-methylnicotinate | HCID 231548 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (6-Methylpyridin-3-yl)methanol | HCID 11228788 | 22.1% |
Reaction Steps
5-Methoxycarbonyl-2-methyl-pyridine (3.0 g, 19.8 mmole) was dissolved in toluene (60 ml) and cooled to -78° C. To this solution, a 39.7 ml of a solution of 1M diisobutylaluminum hydride in toluene was added dropwise. The reaction mixture was stirred for 1 hour at -78° C., allowed to warm to room temperature and stirred for an additional 18 hours. Methanol (8 ml) was then added dropwise at room temperature to the reaction mixture. The mixture was stirred until a thick gel was formed. 1N HCl (10 ml) was added to dissolve the gel. The resulting phases were separated, the organic phase was extracted in ethyl acetate and dried over MgSO4. The solvents were removed yielding crude 5-hydroxymethyl-2-methylpyridine (540 mg) as an oil, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05264437 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-ef3f500433cb4cc3a0d9c6758f3fbccc |
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| Source note | uspto-grants-1993_11 |
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